Ubiquitination/ Proteasome

Ubiquitination/ Proteasome(泛素化/蛋白酶体)

研究方向

Ubiquitination/ Proteasome 相关产品(1292)

  • GC35555 structure
    GC35555Britannin
    CAS: 33627-28-0
    纯度: >99.50%

    Britannin,分离于 Inula aucheriana,是倍半萜内酯。Britannin 通过激活由 ROS 调节的 AMPK 来诱导肝癌细胞凋亡和自噬。Britannin 具有抗增殖和抗炎活性。

  • GC35601 structure
    GC35601CaMKII-IN-1
    CAS: 1208123-85-6
    纯度: >99.50% / >98.00%

    CaMKII-IN-1是一种强效且高度选择性的CaMKII抑制剂,IC 50 值为63nM。

  • GC35613 structure
    GC35613Carvedilol phosphate hemihydrate
    CAS: 610309-89-2

    A β-adrenergic receptor antagonist

  • GC35667 structure
    GC35667CFTR corrector 1
    CAS: 2216712-66-0
    纯度: >99.50%

    An F508del-CFTR corrector and potentiator

  • GC35668 structure
    GC35668CG-200745
    CAS: 936221-33-9

    CG-200745 (CG-200745) 是一种具有口服活性的强效 pan-HDAC 抑制剂,其异羟肟酸部分可与催化袋底部的锌结合。 CG-200745 抑制组蛋白 H3 和微管蛋白的去乙酰化。 CG-200745 诱导 p53 的积累,促进 p53 依赖性反式激活,并增强 MDM2 和 p21 (Waf1/Cip1) 蛋白的表达。 CG-200745 增强了吉西他滨耐药细胞对吉西他滨和 5-氟尿嘧啶 (5-FU;) 的敏感性。 CG-200745 诱导细胞凋亡并具有抗肿瘤作用。

  • GC35812 structure
    GC35812Dasatinib hydrochloride
    CAS: 854001-07-3
    纯度: >98.50% / >99.00%

    An inhibitor of Abl and Src

  • GC35820 structure
    GC35820DDD107498 succinate
    CAS: 2444781-71-7
    纯度: >98.50%

    DDD107498 (M-5717, DDD-498) is a P. falciparum translation elongation factor 2 inhibitor. DDD107498 exhibits a potent and novel spectrum of antimalarial activity against multiple life-cycle stages of the Plasmodium parasite.

  • GC35832 structure
    GC35832Dehydrocorydaline chloride
    CAS: 10605-03-5
    纯度: >98.00%

    An alkaloid with diverse biological activities

  • GC35969 structure
    GC35969eIF4A3-IN-1
    CAS: 2095486-67-0
    纯度: >99.50%

    eIF4A3-IN-1 (compound 53a) 是一种选择性的真核起始因子 4A3 (eIF4A3) 抑制剂 (IC50=0.26 μM; Kd=0.043 μM),eIF4A3-IN-1 与 eIF4A3 的非 ATP 结合位点结合,并在 10 μM 和 3 μM 时明显抑制细胞无义介导的 RNA 衰变 (NMD), 可作为进一步研究 eIF4A3、外显子连接复合体 (EJC) 和 NMD 的探针。

  • GC35982 structure
    GC35982EN6
    CAS: 1808714-73-9
    纯度: >99.00%

    An activator of autophagy

  • GC35998 structure
    GC35998Episilvestrol
    CAS: 697235-39-5
    纯度: >99.50%

    Episilvestrol 是 silvestrol 的衍生物,从 Aglaia silvestris 中分到,能够抑制 eIF4A 靶作用的转录过程。

  • GC36003 structure
    GC36003Erlotinib mesylate
    CAS: 248594-19-6

    An EGFR tyrosine kinase inhibitor

  • GC36023 structure
    GC36023FAAH inhibitor 1
    CAS: 326866-17-5

    FAAH inhibitor 1是一种选择性的、可逆的脂肪酸酰胺水解酶(FAAH)抑制剂,IC 50 值为18±8nM。

  • GC36061 structure
    GC36061Fluvastatin D6 sodium

    An internal standard for the quantification of fluvastatin

  • GC36063 structure
    GC36063FMK 9a
    CAS: 1955550-51-2

    FMK 9a是autophagin-1的抑制剂,在FRET和LRA试验中测定的IC50值分别为80 和73 nM。

  • GC36130 structure
    GC36130Gemcitabine elaidate
    CAS: 210829-30-4
    纯度: >98.00%

    A prodrug form of gemcitabine

  • GC36136 structure
    GC36136Ginkgolide K
    CAS: 153355-70-5
    纯度: >99.50%

    A terpene trilactone with diverse biological activities

  • GC36149 structure
    GC36149GLPG2451
    CAS: 2055015-61-5
    纯度: >99.50%

    GLPG2451 是一种囊性纤维化跨膜电导调节器 (CFTR) 的增强剂,有效增强低温挽救的 F508del CFTR,EC50 为 11.1 nM。

  • GC36163 structure
    GC36163Glycycoumarin
    CAS: 94805-82-0
    纯度: >99.50%

    Glycycoumarin 是一种甘草中主要的生物活性香豆素。Glycycoumarin 通过激活自噬,抑制内质网应激介导的 JNK 和 GSK-3 介导的线粒体途径,来抑制肝细胞脂性凋亡。Glycycoumarin 能直接靶向 T-LAK 细胞源蛋白激酶发挥抗肝癌活性 。

  • GC36215 structure
    GC36215Heparin Lithium salt
    CAS: 9045-22-1
    纯度: 不显示

    Heparin Lithium salt 是一种抗凝剂,可与 抗凝血酶III (ATIII) 可逆地结合 (50-400 U/Kg)。

  • GC36329 structure
    GC36329Irinotecan hydrochloride
    CAS: 100286-90-6
    纯度: >99.00%

    A potent inhibitor of DNA topoisomerase I

  • GC36339 structure
    GC36339Isorhapontigenin
    CAS: 32507-66-7
    纯度: >99.50%

    Isorhapontigenin (ISOR), isolated from Belamcanda chinensis, is a derivative of stilbene. Isorhapontigenin possessed potent antioxidative activity. Isorhapontigenin suppresses interleukin-1β-induced inflammation and cartilage matrix damage in rat chondrocytes.

  • GC36346 structure
    GC36346Isosorbide mononitrate
    CAS: 16051-77-7
    纯度: >99.50%

    A nitric oxide donor with cardioprotective activity

  • GC36356 structure
    GC36356Ixazomib citrate
    CAS: 1239908-20-3
    纯度: >99.50%

    Ixazomib citrate (MLN9708, Ninlaro) is a prodrug of Ixazomib (MLN2238), which is a selective, orally bioavailable inhibitor of 20S proteasome that inhibits the chymotrypsin-like proteolytic (β5) site with IC50 of 3.4 nM and Ki of 0.93 nM, respectively. Ixazomib (MLN2238) also inhibits caspase-like (β1) and trypsin-like (β2) proteolytic sites with IC50 of 31 nM and 3500 nM, respectively.